NO951405L - Substituted N-heteroarylguanidines, their method of preparation, their use as a drug or diagnostic, and drugs containing these - Google Patents

Substituted N-heteroarylguanidines, their method of preparation, their use as a drug or diagnostic, and drugs containing these

Info

Publication number
NO951405L
NO951405L NO951405A NO951405A NO951405L NO 951405 L NO951405 L NO 951405L NO 951405 A NO951405 A NO 951405A NO 951405 A NO951405 A NO 951405A NO 951405 L NO951405 L NO 951405L
Authority
NO
Norway
Prior art keywords
alkyl
perfluoroalkyl
substd
opt
ome
Prior art date
Application number
NO951405A
Other languages
Norwegian (no)
Other versions
NO304426B1 (en
NO951405D0 (en
Inventor
Hans-Werner Kleemann
Hans-Jochen Lang
Jan-Robert Schwark
Andreas Weichert
Wolfgang Scholz
Udo Albus
Original Assignee
Hoechst Ag
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Hoechst Ag filed Critical Hoechst Ag
Publication of NO951405D0 publication Critical patent/NO951405D0/en
Publication of NO951405L publication Critical patent/NO951405L/en
Publication of NO304426B1 publication Critical patent/NO304426B1/en

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
    • C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
    • C07D401/12—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings linked by a chain containing hetero atoms as chain links
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P11/00—Drugs for disorders of the respiratory system
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P13/00—Drugs for disorders of the urinary system
    • A61P13/02—Drugs for disorders of the urinary system of urine or of the urinary tract, e.g. urine acidifiers
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P15/00—Drugs for genital or sexual disorders; Contraceptives
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00—Drugs for disorders of the nervous system
    • A61P25/28—Drugs for disorders of the nervous system for treating neurodegenerative disorders of the central nervous system, e.g. nootropic agents, cognition enhancers, drugs for treating Alzheimer's disease or other forms of dementia
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00—Antineoplastic agents
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00—Drugs for disorders of the cardiovascular system
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00—Drugs for disorders of the cardiovascular system
    • A61P9/06—Antiarrhythmics
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00—Drugs for disorders of the cardiovascular system
    • A61P9/08—Vasodilators for multiple indications
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00—Drugs for disorders of the cardiovascular system
    • A61P9/10—Drugs for disorders of the cardiovascular system for treating ischaemic or atherosclerotic diseases, e.g. antianginal drugs, coronary vasodilators, drugs for myocardial infarction, retinopathy, cerebrovascula insufficiency, renal arteriosclerosis
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00—Drugs for disorders of the cardiovascular system
    • A61P9/12—Antihypertensives
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D207/00—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom
    • C07D207/02—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
    • C07D207/30—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having two double bonds between ring members or between ring members and non-ring members
    • C07D207/34—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having two double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D307/00—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom
    • C07D307/02—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings
    • C07D307/34—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
    • C07D307/56—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • C07D307/68—Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D333/00—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom
    • C07D333/02—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom not condensed with other rings
    • C07D333/04—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom not condensed with other rings not substituted on the ring sulphur atom
    • C07D333/26—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom not condensed with other rings not substituted on the ring sulphur atom with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • C07D333/38—Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
    • C07D403/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
    • C07D403/12—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings linked by a chain containing hetero atoms as chain links
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D405/00—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
    • C07D405/02—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings
    • C07D405/12—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings linked by a chain containing hetero atoms as chain links
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D409/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms
    • C07D409/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings
    • C07D409/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings linked by a chain containing hetero atoms as chain links

Landscapes

  • Organic Chemistry (AREA)
  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Veterinary Medicine (AREA)
  • Public Health (AREA)
  • General Chemical & Material Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Cardiology (AREA)
  • Heart & Thoracic Surgery (AREA)
  • Urology & Nephrology (AREA)
  • Neurology (AREA)
  • Biomedical Technology (AREA)
  • Neurosurgery (AREA)
  • Vascular Medicine (AREA)
  • Hospice & Palliative Care (AREA)
  • Psychiatry (AREA)
  • Endocrinology (AREA)
  • Reproductive Health (AREA)
  • Pulmonology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
  • Medicines Containing Antibodies Or Antigens For Use As Internal Diagnostic Agents (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Furan Compounds (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Pyrrole Compounds (AREA)
  • Agricultural Chemicals And Associated Chemicals (AREA)
  • Heterocyclic Compounds Containing Sulfur Atoms (AREA)
  • Pyridine Compounds (AREA)

Abstract

Heteroaryl-guanidine derivs. of formula (I) and their salts are new. A = S(O)m, O or NR5; m = 0, 1 or 2; R5 = H, 1-8C alkyl or CmH2mR81; R81 = 3-8C cycloalkyl, phenyl (opt. substd. by 1-3 of F, Cl, CF3, Me, OMe, and NR82R83) or 1-9C heteroaryl (bonded via C or N and opt. substd. by 1-3 of F, Cl, CF3, Me, OMe, OH, NH2, NHMe and NMe2); R82, R83 = H or Me; one of R1, R2 = CO-N=C(NH2)2; the other = H, F, Cl, Br, I, 1-3C alkyl, OR6, 1-4C perfluoroalkyl, CO-N=C(NH2)2 or NR6R7; R6,R7 = H or 1-3C alkyl; R3, R4 = (i) H, F, Cl, Br, I, CN, X(CH2)m(1-6C) perfluoroalkyl, X(CH2)mF, S(O)mR8, CONR9R10, COR11, SO2NR12R13; (ii) 1-8C alkyl, CmH2mR81; (iii) 1-9C heteroaryl (opt. substd. by 1-3 of F, Cl, CF3, Me, OMe, OH, NH2, NHMe and NMe2); (iv) -Y-C6H4-(CO)i-(CHOH)j-(CHOH)k-R23; (v) H, F, Cl, Br, I, CN, 1-8C alkyl, 1-8C perfluoralkyl, 3-8C alkenyl, CgH2g-R26; SR29, OR30, NR31R32, CR33R34R35; (vii) -W-C6H4-R97; (viii) S(O)mR37, SO2NR38R39; (ix) X1R46; (x) SR64, OR65, NHR66, NR67R68, CHR_R69R70, CR54R55-OH, C IDENTICAL C-R56 C(R58) C-R57 (sic), (CR59R60)u-CO-(CR61R62)v-R63; (xi) SO2NHR76; or (xii)NR84R85; X = O, S or NR14; R14 = H or 1-3C alkyl; R8 = 1-5C alkyl, 3-6C alkenyl, CnH2nR15 or CF3; R9, R11, R12 = H or as R8; n = 0-4; R15 = 3-7C cycloalkyl or phenyl (opt. substd. by 1-3 of F, Cl, CF3, Me, OMe and NR16R17); R16,R17 = H or 1-4C alkyl; R10, R13 = H or 1-4C alkyl; or R9+R10 or R12+R13 = (CH2)4 or (CH2)5 in which one CH2 may be replaced by O, S, NH, NMe or N-benzyl; R18 = 3-8C cycloalkyl or phenyl (opt. substd. by 1-3 of F, Cl, CF3, Me, OMe and NR19R20); R19,R20 = H or Me; Y = O, S or NR22; h = 0 or 1; i, j, k = 0-4; provided that h, i and k are not all 0; R22,R23 = H or 1-3C alkyl; g = 0-4; R26 = 3-8C cycloalkyl, phenyl, biphenyl, or naphthyl (where aromatics are opt. substd. by 1-3 of F, Cl, CF3, Me, OMe and NR27R28); R27,R28 = H, 1-4C alkyl or 1-4C perfluoroalkyl; R29-R31, R33 = -(CH2)m- (1-9C) heteroaryl (opt. substd. as in R81); R32, R34 , R35 = H, 1-4C alkyl, 1-4C perfluoroalkyl, or as R29; R96 = heteroaryl as defined for R81, or benzyl; W = O, S or NR36; R36 = H or 1-4C alkyl; R37 = 1-8C alkyl, 1-8C perfluoroalkyl, 3-8C alkenyl or -CsH2s-R40; s = 0-4; R40 = as R26; R38 = H, 1-8C alkyl, 1-8C perfluoroalkyl, 3-8C alkenyl or -CwH2w-R26; R39 = H, 1-4C alkyl or 1-4C perfluoroalkyl; or R38+R39 = (CH2)4 or (CH2)5, in which one CH2 may be replaced by O, S, NH, NMe or N-benzyl; X1 = O, S, NR47, (D=O)A'- or NR48C=MN*(R49)-; M = O or S; A' = O or NR50; D = C or SO; R46, R49 = 1-8C alkyl, 3-8C alkenyl, -(CH2)b-(1-7C)perfluoroalkyl or -CxH2x-R26; b = 0 or 1; x = 0-4; R47, R48, R50 = H, 1-4C alkyl or 1-4C perfluoroalkyl; or R46+R47 or R46+R48 = (CH2)4 or (CH2)5 in which CH2 may be replaced by O, S, NH, NMe or N-benzyl; A' and N* are bonded to the phenyl ring of the benzoylguanidine structure; R64-R67, R69 = -(CH2)y-(CHOH)z-(CH2)q'-(CH2OH)t-R71 or -(CH2)b'-O-(CH2CH2O)c'-R72; R71, R72 = H or Me; b', c' are not defined; u, t = 1-4; v, y, z, a' = 0-4; R68, R70, R54, R55 = H or 1-6C alkyl; or CR69R70 or CR54R55 = 3-8C cycloalkylidene; R63 = H, 1-6C alkyl, 3-8C cycloalkyl or -CeH2e-R73; e = 0-4; R80 = 5-7C cycloalkyl or phenyl (opt. substd. by 1-3 of F, Cl, CF3, OMe and 1-4C alkyl); or R77+R78 = (CH2)4 or (CH2)5, in which one CH2 may be replaced by O, S, NH, NMe or N-benzyl; R79 = as R77; or amidino; R84, R85 = H or 1-4C alkyl; or R84+R85 = (CH2)4 or (CH2)5 in which one CH2 may be replaced by O, S, NH, NMe or N-benzyl or 1 or 2 CH2 gps. may be replaced by CH-Cd_'H2d'+1; d' is not defined. Cpds. (I; A = O; R1 = -CON=C(NH2)2; R2, R3 = H; R4 = H, Me or Et) are excluded.
NO951405A 1994-04-11 1995-04-10 Substituted 4-heteroaroylguanidines, their use in the manufacture of drugs or diagnostics and drugs containing these NO304426B1 (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
DE4412334A DE4412334A1 (en) 1994-04-11 1994-04-11 Substituted N-heteroaroylguanidines, process for their preparation, their use as a medicament or diagnostic agent, and medicament containing them

Publications (3)

Publication Number Publication Date
NO951405D0 NO951405D0 (en) 1995-04-10
NO951405L true NO951405L (en) 1995-10-12
NO304426B1 NO304426B1 (en) 1998-12-14

Family

ID=6515052

Family Applications (1)

Application Number Title Priority Date Filing Date
NO951405A NO304426B1 (en) 1994-04-11 1995-04-10 Substituted 4-heteroaroylguanidines, their use in the manufacture of drugs or diagnostics and drugs containing these

Country Status (16)

Country Link
US (1) US5698581A (en)
EP (1) EP0676395B1 (en)
JP (1) JP4171078B2 (en)
CN (1) CN1073988C (en)
AT (1) ATE248817T1 (en)
AU (1) AU683722B2 (en)
CA (1) CA2146707C (en)
DE (2) DE4412334A1 (en)
ES (1) ES2206471T3 (en)
FI (1) FI951681A (en)
HU (1) HUT71616A (en)
IL (1) IL113310A (en)
NO (1) NO304426B1 (en)
NZ (1) NZ270894A (en)
TW (1) TW349941B (en)
ZA (1) ZA952930B (en)

Families Citing this family (39)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE19540995A1 (en) * 1995-11-03 1997-05-07 Hoechst Ag Substituted sulfonimidamides, process for their preparation, their use as a medicament or diagnostic agent, and medicament containing them
DE19542306A1 (en) * 1995-11-14 1997-05-15 Hoechst Ag Sulfonylamino-substituted benzoylguanidines, process for their preparation, their use as a medicament or diagnostic agent, and medicament containing them
PL316439A1 (en) * 1995-11-20 1997-05-26 Hoechst Ag Novel substituted derivatives of benzoyloguanidine, method of obtaining them, their application in production of pharmaceutic and diagnostic agents and pharmaceutic agent as such
DE19546736A1 (en) * 1995-12-14 1997-06-19 Hoechst Ag Substituted chromanylsulfonyl (thio) ureas, process for their preparation and their use in the manufacture of pharmaceutical preparations
DE19548708A1 (en) * 1995-12-23 1997-06-26 Merck Patent Gmbh Cyclic sulfones
CA2195697A1 (en) * 1996-02-02 1997-08-03 Masahumi Kitano Novel substituted guanidine derivatives, process for production thereof, and pharmaceutical uses thereof
DE19605610A1 (en) * 1996-02-15 1997-08-21 Hoechst Ag Substituted thiophenylalkenylcarboxylic acid guanidides, processes for their preparation, their use as medicaments or diagnostic agents and medicaments containing them
US6136984A (en) * 1996-04-22 2000-10-24 Novo Nordisk A/S Solid phase and combinatorial synthesis of substituted thiophenes and of arrays of substituted thiophenes
JPH09291076A (en) * 1996-04-24 1997-11-11 Sumitomo Pharmaceut Co Ltd Substituted guanidine derivative and its production
US6344476B1 (en) 1997-05-23 2002-02-05 Bayer Corporation Inhibition of p38 kinase activity by aryl ureas
US6187799B1 (en) 1997-05-23 2001-02-13 Onyx Pharmaceuticals Inhibition of raf kinase activity using aryl ureas
US5994396A (en) * 1997-08-18 1999-11-30 Centaur Pharmaceuticals, Inc. Furansulfonic acid derivatives and pharmaceutical compositions containing the same
US7329670B1 (en) 1997-12-22 2008-02-12 Bayer Pharmaceuticals Corporation Inhibition of RAF kinase using aryl and heteroaryl substituted heterocyclic ureas
US7517880B2 (en) 1997-12-22 2009-04-14 Bayer Pharmaceuticals Corporation Inhibition of p38 kinase using symmetrical and unsymmetrical diphenyl ureas
EP1454902A1 (en) * 1998-02-27 2004-09-08 Pfizer Products Inc. N- (substituted five-membered di-or triaza diunsaturated ring)carbonyl guanidine derivateives for the treatment of ischemia
US8124630B2 (en) 1999-01-13 2012-02-28 Bayer Healthcare Llc ω-carboxyaryl substituted diphenyl ureas as raf kinase inhibitors
EP1140840B1 (en) 1999-01-13 2006-03-22 Bayer Pharmaceuticals Corp. -g(v)-carboxyaryl substituted diphenyl ureas as raf kinase inhibitors
EP1158985B1 (en) 1999-01-13 2011-12-28 Bayer HealthCare LLC OMEGA-CARBOXY ARYL SUBSTITUTED DIPHENYL UREAS AS p38 KINASE INHIBITORS
RU2319693C9 (en) 1999-01-13 2008-08-20 Байер Копэрейшн Derivatives of urea (variants), pharmaceutical composition (variants) and method for treatment of diseases associated with cancer cells growth (variants)
US7928239B2 (en) 1999-01-13 2011-04-19 Bayer Healthcare Llc Inhibition of RAF kinase using quinolyl, isoquinolyl or pyridyl ureas
DE10061876A1 (en) 2000-12-12 2002-06-20 Aventis Pharma Gmbh Arylated furan and thiophene carboxamides, processes for their preparation, their use as medicaments and pharmaceutical preparations containing them
US7235576B1 (en) 2001-01-12 2007-06-26 Bayer Pharmaceuticals Corporation Omega-carboxyaryl substituted diphenyl ureas as raf kinase inhibitors
US7371763B2 (en) 2001-04-20 2008-05-13 Bayer Pharmaceuticals Corporation Inhibition of raf kinase using quinolyl, isoquinolyl or pyridyl ureas
EP1478358B1 (en) 2002-02-11 2013-07-03 Bayer HealthCare LLC Sorafenib tosylate for the treatment of diseases characterized by abnormal angiogenesis
WO2003068229A1 (en) 2002-02-11 2003-08-21 Bayer Pharmaceuticals Corporation Pyridine, quinoline, and isoquinoline n-oxides as kinase inhibitors
AU2003209118A1 (en) 2002-02-11 2003-09-04 Bayer Pharmaceuticals Corporation Aryl ureas as kinase inhibitors
US6803379B2 (en) * 2002-06-04 2004-10-12 Jose A. Fernandez-Pol Pharmacological agents and methods of treatment that inactivate pathogenic prokaryotic and eukaryotic cells and viruses by attacking highly conserved domains in structural metalloprotein and metalloenzyme targets
FR2842524B1 (en) * 2002-07-16 2005-04-22 Aventis Pharma Sa PHARMACEUTICAL COMPOSITIONS CONTAINING 3-GUANIDINOCARBONYL-1-HETEROARYL-PYRROLE DERIVATIVE, PROCESS FOR PREPARING THE SAME AS MEDICAMENTS
CN1308323C (en) * 2002-07-24 2007-04-04 三井化学株式会社 Process for producing 2-alkyl-3-aminothiophene derivative
ATE440827T1 (en) * 2002-12-04 2009-09-15 Ore Pharmaceuticals Inc MELANOCORTIN RECEPTOR MODULATORS
UY28213A1 (en) 2003-02-28 2004-09-30 Bayer Pharmaceuticals Corp NEW CYANOPIRIDINE DERIVATIVES USEFUL IN THE TREATMENT OF CANCER AND OTHER DISORDERS.
CA2526636C (en) 2003-05-20 2012-10-02 Bayer Pharmaceuticals Corporation Diaryl ureas for diseases mediated by pdgfr
CL2004001834A1 (en) 2003-07-23 2005-06-03 Bayer Pharmaceuticals Corp COMPOUND 4- {4- [3- (4-CHLORO-3-TRIFLUOROMETILFENIL) -UREIDO] -3-FLUOROFENOXI} -PIRIDIN-2-METHYLAMIDE, RAF INHIBITOR, VEGFR, P38 AND PDGFR KINASES, ITS SALTS; PHARMACEUTICAL COMPOSIICON; PHARMACEUTICAL COMBINATION; AND ITS USE TO TREAT HYPERPROL DISORDERS
MXPA06013118A (en) * 2004-05-12 2007-02-28 Schering Corp Cxcr1 and cxcr2 chemokine antagonists.
DE102006027229A1 (en) * 2006-06-09 2007-12-20 Grünenthal GmbH 1,3-Disubstituted 4-methyl-1H-pyrrole-2-carboxylic acid amides and their use for the preparation of medicaments
US20100113421A1 (en) * 2006-10-06 2010-05-06 Williams Theresa M Non-nucleoside reverse transcriptase inhibitors
CN102482249B (en) 2009-07-08 2016-06-08 德米拉(加拿大)公司 For treating the TOFA analog of skin disorder or morbid state
EP2602248A1 (en) 2011-12-05 2013-06-12 University Of Leicester Novel pyrrole compounds
RU2631011C1 (en) * 2016-07-12 2017-09-15 Федеральное государственное бюджетное образовательное учреждение высшего образования "Омский государственный технический университет" Device for generating directional inertial force

Family Cites Families (24)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
IT1053674B (en) * 1968-01-31 1981-10-10 Istituto Farmacobiologico Sero N AMIDINO OXYZOLIC CARBOXYAMES WITH NATRIURETIC ACTION
FR2027285A1 (en) * 1968-12-29 1970-09-25 Dainippon Pharmaceutical Co Pharmaceutical derivs of 4-nitropyrrol-2- - carboxylic acid amides
BE758762A (en) * 1969-11-12 1971-04-16 Shionogi & Cy Ltd ISOXAZOLE DERIVATIVES AND THEIR PREPARATION
FR2073284B1 (en) * 1969-12-23 1973-07-13 Ferlux
SU380651A1 (en) * 1971-05-11 1973-05-15 вители Саратовский государственный университет имени Н. Г. Чернышевского , Саратовский государственный медицинский институт METHOD FOR OBTAINING GUANIDIDES OF FURANCARBONE OR TETRAGYDROFURANKARBONIC ACIDS
US4894376A (en) * 1988-02-26 1990-01-16 Trustees Of The University Of Pennsylvania Methods of treating diseases characterized by hyperexcitability of neurons
US5002965A (en) * 1989-05-09 1991-03-26 Societe De Conseils De Recherches Et D'applications Scientifiques (S.C.R.A.S.) Use of ginkgolides to prevent reperfusion injury in organ transplantation
DE3929582A1 (en) * 1989-09-06 1991-03-07 Hoechst Ag BENZOYLGUANIDINE, METHOD FOR THE PRODUCTION THEREOF, THEIR USE AS A MEDICINE AND THE MEDICINE CONTAINING IT
TW213903B (en) * 1991-08-16 1993-10-01 Boehringer Ingelheim Kg
CZ284456B6 (en) * 1992-02-15 1998-12-16 Hoechst Aktiengesellschaft Amino substituted benzylguanidines, process of their preparation and their use for preparing medicaments
EP0556674B1 (en) * 1992-02-15 1996-06-19 Hoechst Aktiengesellschaft 3,5-substituted benzoylguanidines with antiarrhythmic activity and cell proliferation inhibiting activity
EP0556673B1 (en) * 1992-02-15 1997-09-17 Hoechst Aktiengesellschaft Ortho-substituted benzoylguanidines, process for their preparation, their use as medicament or diagnostic agent, as well as medicaments containing them
ES2092729T3 (en) * 1992-07-01 1996-12-01 Hoechst Ag 3,4,5-SUBSTITUTED BENZOYLGUANIDINES, PROCEDURE FOR THEIR PREPARATION, USE AS A MEDICINAL PRODUCT OR DIAGNOSTIC AGENT, AS WELL AS A MEDICINAL PRODUCT CONTAINING THEM.
ES2097409T3 (en) * 1992-09-22 1997-04-01 Hoechst Ag BENZOILGUANIDINES, PROCEDURE FOR ITS PREPARATION, AS WELL AS ITS USE AS ANTIARRHYTHMIC.
EP0590455B1 (en) * 1992-09-28 2000-12-27 Hoechst Aktiengesellschaft Antiarrhythmic and cardioprotective substituted 1(2H)-isoquinolines, process for their production, medicament containing them and their use for the production of a medicament for combating heart failures
US5260091A (en) * 1992-10-21 1993-11-09 Interneuron Pharmaceuticals Inc. Salt taste enhancers
DK0603650T3 (en) * 1992-12-16 1997-10-20 Hoechst Ag 3,5-Substituted aminobenzoylguanidines, their method of preparation, their use as a drug or diagnostic, and drug containing them.
CA2121391A1 (en) * 1993-04-28 1994-10-29 Atsuyuki Kojima Indoloylguanidine derivatives
EP0639573A1 (en) * 1993-08-03 1995-02-22 Hoechst Aktiengesellschaft Benzocondensed five membered heterocycles, process of their preparation, their use as drug, as diagnostic means and pharmaceuticals containing it
DE4327244A1 (en) * 1993-08-13 1995-02-16 Hoechst Ag Urea-substituted benzoyl guanedines, process for their preparation, their use as a medicament or diagnostic agent, and medicament containing them
DE4344550A1 (en) * 1993-12-24 1995-06-29 Hoechst Ag Substituted 1-oxo-1,2-dihydro-isoquinolinoyl and 1,1-dioxo-2H-1,2-benzothiazinoylguanidines, processes for their preparation, their use as medicaments or diagnostic agents, and medicaments containing them
TW415937B (en) * 1994-01-25 2000-12-21 Hoechst Ag Phenyl-substituted alkylcarboxylic acid guanidides bearing perfluoroalkyl groups, process for their preparation, their use as a medicament or diagnostic, and medicament containing them
DE4417004A1 (en) * 1994-05-13 1995-11-16 Hoechst Ag Perfluoroalkyl-substituted benzoylguanidines, process for their preparation, their use as a medicament or diagnostic agent, and medicament containing them
DE4432101A1 (en) * 1994-09-09 1996-03-14 Hoechst Ag Amino acid-substituted benzoylguanidines, process for their preparation, their use as a medicament or diagnostic agent, and medicament containing them

Also Published As

Publication number Publication date
CA2146707C (en) 2008-10-21
EP0676395A3 (en) 1996-03-06
JP4171078B2 (en) 2008-10-22
DE4412334A1 (en) 1995-10-19
JPH07291927A (en) 1995-11-07
AU1635495A (en) 1995-10-19
EP0676395A2 (en) 1995-10-11
NO304426B1 (en) 1998-12-14
NZ270894A (en) 1997-09-22
HUT71616A (en) 1996-01-29
FI951681A0 (en) 1995-04-07
ES2206471T3 (en) 2004-05-16
IL113310A (en) 2000-06-29
ZA952930B (en) 1996-01-26
ATE248817T1 (en) 2003-09-15
TW349941B (en) 1999-01-11
NO951405D0 (en) 1995-04-10
CA2146707A1 (en) 1995-10-12
CN1117044A (en) 1996-02-21
CN1073988C (en) 2001-10-31
HU9501035D0 (en) 1995-06-28
IL113310A0 (en) 1995-07-31
AU683722B2 (en) 1997-11-20
FI951681A (en) 1995-10-12
US5698581A (en) 1997-12-16
EP0676395B1 (en) 2003-09-03
DE59510782D1 (en) 2003-10-09

Similar Documents

Publication Publication Date Title
NO951405D0 (en) Substituted N-heteroarylguanidines, their method of preparation, their use as a drug or diagnostic, and drugs containing these
Harvey et al. Excitatory acidic amino acids and the cation content and sodium ion flux of isolated tissues from the brain
AR059956A1 (en) PHENETALONAMINE DERIVATIVES, PREPARATION PROCESSES AND PHARMACEUTICAL COMPOSITIONS CONTAINING THEM
KR960010639A (en) Imidazopyridine derivatives
PE20040949A1 (en) DERIVATIVES OF HEXAHIDRO-PIRAZINO [1,2-a] PIRIMIDIN-4,7-DIONA SUBSTITUTED IN POSITION 3 BY NITROGEN AND PROCEDURE FOR THE PREPARATION OF THE PHARMACEUTICAL COMPOSITION
ATE166056T1 (en) GALLIUM III COMPLEXES, METHOD FOR THE PRODUCTION THEREOF AND PHARMACEUTICAL COMPOSITIONS CONTAINING THEM
NO964639D0 (en) Substituted sulfonimidamides, their method of preparation, their use as a medicament or diagnostic, and medicament containing the compound
ES2131241T3 (en) SUBSTITUTED BENZOYLGUANIDINES, PROCEDURE FOR THEIR PREPARATION, USE AS A MEDICINAL PRODUCT OR DIAGNOSTIC AGENT, AS WELL AS A MEDICINAL PRODUCT CONTAINING THEM.
DK163126C (en) 1-ETHYL-1,4-DIHYDRO-4-OXO-3-CARBOXY-QUINOLINE OR (1,8-NAPHTHYRIDINE) DERIVATIVES, PROCEDURES FOR PREPARING THEREOF, PHARMACEUTICAL PREPARATIONS CONTAINING THOSE INCLUDING THIS PART
DK0623138T3 (en) New adenosine derivatives, processes for their preparation and pharmaceutical compositions containing them
Rubin et al. Fulminant hepatic failure caused by genital herpes in a healthy person
Williams et al. Hemolytic activity of Borrelia burgdorferi
Lewis et al. Pure red cell hypoplasia secondary to isoniazid
Gangarosa Epidemiology of Escherichia coli in the United States
ES2097926T3 (en) USE OF ACID DERIVATIVES 1,3,5-TRIAZIN-2,4,6-TRIS-ALKYLAMINOCARBOXYLICS AS BIOCIDAL AGENTS.
Yachnin et al. Role of Calcium in Complement Dependent Hemolysis.
Gerke et al. Leptospirosis-3 cases and a review
DK146589A (en) Means for the preservation or re-establishment of the skin's health
DK0897919T3 (en) New pyridonecarboxylic acid derivatives or salts thereof and antibacterial agents containing them as the active ingredient
FI955670A0 (en) 2-Aminobenzenesulfonic acid and 2-aminobenzenesulfonyl chloride derivatives, their preparation and use as synthesis intermediates
Stuart Comparison of rifampicin and tetracycline based regimens in the treatment of experimental brucellosis
Winn Jr Cellular inflammatory defenses in Legionella pneumonia
Rubinacci et al. Ca2+ transport and permeability in inside-out red cell membrane vesicles after freezing
AR038837A1 (en) USE OF INHIBITORS OF THE CHLORIDE / BICARBONATE SODIUM EXCHANGER FOR THE TREATMENT OF THROMBOTIC AND INFLAMMATORY DISORDERS
Sanders Allogeneic Marrow Transplantation for Acute Leukemia

Legal Events

Date Code Title Description
MM1K Lapsed by not paying the annual fees